| Product NDC: | 57520-0303 | 
| Proprietary Name: | Renaforce | 
| Non Proprietary Name: | Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, | 
| Active Ingredient(s): | 3; 3; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 57520-0303 | 
| Labeler Name: | Apotheca Company | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC | 
| Start Marketing Date: | 20101102 | 
| Package NDC: | 57520-0303-1 | 
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0303-1) | 
| NDC Code | 57520-0303-1 | 
| Proprietary Name | Renaforce | 
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0303-1) | 
| Product NDC | 57520-0303 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Berberis vulgaris, Echinacea angustifolia, Coccus cacti, Kali muriaticum, Lycopodium clavatum, Nitricum acidum, | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20101102 | 
| Marketing Category Name | UNAPPROVED HOMEOPATHIC | 
| Labeler Name | Apotheca Company | 
| Substance Name | BERBERIS VULGARIS ROOT BARK; ECHINACEA ANGUSTIFOLIA; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; POTASSIUM CHLORIDE; PROTORTONIA CACTI | 
| Strength Number | 3; 3; 12; 12; 12; 12 | 
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL | 
| Pharmaceutical Classes |